生物来源
mouse
偶联物
unconjugated
抗体形式
ascites fluid
抗体产品类型
primary antibodies
克隆
CALD-5, monoclonal
包含
15 mM sodium azide
种属反应性
human, chicken
技术
indirect immunofluorescence: suitable using frozen human tissue sections
microarray: suitable
western blot: 1:100 using chicken gizzard extract
同位素/亚型
IgG1
UniProt登记号
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... CALD1(800)
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免疫原
caldesmon from turkey gizzard
生化/生理作用
The antibody localizes the high molecular weight form of caldesmon in chicken or turkey gizzard and the low molecular weight form of caldesmon in chicken fibroblasts by immunoblotting. CALD-5 localizes both the high and low molecular weight caldesmons in cultured human smooth muscle cells. The antibody reacts with epitopes located on the N-terminal, non-calmodulin-binding part of caldesmon.
免责声明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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W Durand-Arczynska et al.
Histochemistry, 100(6), 465-471 (1993-12-01)
Calponin and caldesmon are two proteins considered to play a regulatory role in smooth muscle contraction, which have never previously been found to be expressed in subcultured cells. In the present study, immunocytochemistry and immunoblotting were performed to identify these
Javier Kattan et al.
Developmental dynamics : an official publication of the American Association of Anatomists, 230(1), 34-43 (2004-04-27)
To study the formation of the coronary vessels in the developing avian heart, we stained developmentally staged quail hearts with the endothelial specific antibody QH-1. QH-1 reacted with individual cells in the proepicardial organ in Hamburger and Hamilton stage (HH)
W Rozek et al.
Polish journal of veterinary sciences, 16(4), 663-669 (2013-01-01)
Changes in the level of cellular proteins in cells inoculated with equine influenza virus H7N7 and H3N8 were studied with microarray technique. H3N8 induced pro-apoptotic proteins while H7N7 induced both pro- as well as anti-apoptotic factors. The higher level of
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